Department of Biomedical Engineering, College of Engineering, University of Michigan, Ann Arbor, Michigan 48109, USA.
Department of Mechanical Engineering, College of Engineering, University of Michigan, Ann Arbor, Michigan 48109, USA ; Mobility and Thermal Management Department, General Dynamics Land Systems, Sterling Heights, Michigan 48310, USA.
Biomicrofluidics. 2014 Feb 25;8(1):016503. doi: 10.1063/1.4865855. eCollection 2014 Jan.
We present a microfluidic device designed for maintenance and culture of non-adherent mammalian cells, which enables both recirculation and refreshing of medium, as well as easy harvesting of cells from the device. We demonstrate fabrication of a novel microfluidic device utilizing Braille perfusion for peristaltic fluid flow to enable switching between recirculation and refresh flow modes. Utilizing fluid flow simulations and the human promyelocytic leukemia cell line, HL-60, non-adherent cells, we demonstrate the utility of this RECIR-REFRESH device. With computer simulations, we profiled fluid flow and concentration gradients of autocrine factors and found that the geometry of the cell culture well plays a key role in cell entrapping and retaining autocrine and soluble factors. We subjected HL-60 cells, in the device, to a treatment regimen of 1.25% dimethylsulfoxide, every other day, to provoke differentiation and measured subsequent expression of CD11b on day 2 and day 4 and tumor necrosis factor-alpha (TNF-α) on day 4. Our findings display perfusion sensitive CD11b expression, but not TNF-α build-up, by day 4 of culture, with a 1:1 ratio of recirculation to refresh flow yielding the greatest increase in CD11b levels. RECIR-REFRESH facilitates programmable levels of cell differentiation in a HL-60 non-adherent cell population and can be expanded to other types of non-adherent cells such as hematopoietic stem cells.
我们提出了一种用于维持和培养非贴壁哺乳动物细胞的微流控装置,该装置能够实现培养基的再循环和更新,并且便于从装置中收获细胞。我们展示了一种利用盲文灌注实现蠕动流的新型微流控装置的制造方法,从而能够在再循环和更新流动模式之间进行切换。利用流体流动模拟和人早幼粒细胞白血病细胞系 HL-60 非贴壁细胞,我们证明了这种 RECIR-REFRESH 装置的实用性。通过计算机模拟,我们对细胞培养腔内的流体流动和自分泌因子的浓度梯度进行了分析,发现细胞培养腔的几何形状在细胞捕获和保留自分泌和可溶性因子方面起着关键作用。我们将 HL-60 细胞置于装置中,每隔一天用 1.25%的二甲基亚砜处理,以诱导分化,并在第 2 天和第 4 天测量 CD11b 的表达,在第 4 天测量肿瘤坏死因子-α(TNF-α)的表达。我们的研究结果显示,在培养的第 4 天,通过灌注敏感的 CD11b 表达,但 TNF-α没有积累,再循环与更新流动的 1:1 比例使 CD11b 水平的增加最大。RE CIR-REFRESH 促进了 HL-60 非贴壁细胞群中可编程水平的细胞分化,并且可以扩展到其他类型的非贴壁细胞,如造血干细胞。